Global Site Identification and Feasibility Specialist Posted Date 23 hours ago(1/14/2025 10:03 AM) ID 2025-116332 Location : Location US-Remote Overview

As a Global Site Identification and Feasibility Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

What you will be doing:

Work with clinical study teams to ensure the accuracy of data in CTMS.Provide support, under the direction of the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist, to clinical systems end users, including receipt, evaluation and recommendation for all issue/enhancement requests.Conduct research and data analysis to identify potential sites that meet the study criteria and objectivesAssist with feasibility launch to include system set-up, feasibility questionnaire creation and site-level feasibility questionnaire outreach.Effectively communicating with study teams and relevant stakeholders as needed to coordinate and support additional feasibility activities as identified by the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility SpecialistTracking and data entry of feasibility responses and reporting responses to the internal stakeholders.Troubleshoot any issues or discrepancies that arise in the feasibility process (in-house and/or outsourced studies)Stay up-to-date with current regulations and industry trends related to site feasibilitySupporting enrollment forecasting and discussing scenarios with internal or external stakeholders under the supervision of the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist Qualifications

You are:

 

B.S. in a scientific or allied health field (or equivalent degree) and 3+ years of experience demonstrating thorough understanding of clinical trial conduct and processes and/or 2+ years of feasibility/recruitmentExperience with trial optimization vendors, tools, and methodsAnalytical thinker with great attention to detail;Good knowledge of concepts of clinical research and drug developmentExperience collaborating with internal and external stakeholdersAbility to prioritize multiple projects and tasks within tight timelines;Excellent written and verbal communication skills.Demonstrated administrative and project management abilities in an academic, CRO or sponsor environment

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

Various annual leave entitlementsA range of health insurance offerings to suit you and your family’s needsCompetitive retirement planning offerings to maximise savings and plan with confidence for the years aheadGlobal Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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